From: | "Mauricio Avigdor" |
Greetings: I am having a bit of difficulty with an immunofluorescence protocol (IF). I am using fresh tissue fixed for 10 minutes in cold acetone. Are there any fixatives that are well suited to IF protocols? Has anyone attempted to stain unfixed tissue? _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet |